Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1780004-1780338 | Common:1; Rare:62 | ||||
chr1:1780415-1780705 | Common:2; Rare:49 | ||||
chr1:1889960-1890154 | Rare:65 | ||||
chr1:1891134-1891554 | Common:3; Rare:102 | ||||
chr1:1919231-1919457 | Rare:93 | ||||
chr1:1919653-1919781 | Common:3; Rare:44 | ||||
chr1:2050105-2050505 | Common:2; Rare:166 | ||||
chr1:2194640-2194876 | Rare:76 | ||||
chr1:2195013-2195153 | Rare:26 | ||||
chr1:2195213-2195246 | Rare:3 | ||||
chr1:2195264-2195450 | Rare:45 | ||||
chr1:2199188-2199628 | Rare:92 | ||||
chr1:2229176-2229289 | Common:1; Rare:35; Clinvar:3; Clinvar (benign):5 | ||||
chr1:2391474-2391926 | Common:2; Rare:163 | ||||
chr1:2412234-2412396 | Rare:50 |